Gerssen-Schoorl KB[au] - Search Results

Year	Number of Results
1988	2
1989	1
1990	1
1994	1
1995	1
1997	1
1998	1
1999	1
2005	2
2006	1
2007	1
2008	1
2009	1
2010	1
2023	0

1

Paracentric inversion inv(11)(q21q23) in The Netherlands.

Madan K, Pieters MH, Kuyt LP, van Asperen CJ, de Pater JM, Hamers AJ, Gerssen-Schoorl KB, Hustinx TW, Breed AS, Van Hemel JO, et al. Madan K, et al. Among authors: gerssen schoorl kb. Hum Genet. 1990 Jun;85(1):15-20. doi: 10.1007/BF00276319. Hum Genet. 1990. PMID: 2358301

2

Selective chromosome analysis in couples with two or more miscarriages: case-control study.

Franssen MT, Korevaar JC, Leschot NJ, Bossuyt PM, Knegt AC, Gerssen-Schoorl KB, Wouters CH, Hansson KB, Hochstenbach R, Madan K, van der Veen F, Goddijn M. Franssen MT, et al. Among authors: gerssen schoorl kb. BMJ. 2005 Jul 16;331(7509):137-41. doi: 10.1136/bmj.38498.669595.8F. Epub 2005 Jun 28. BMJ. 2005. PMID: 15985440 Free PMC article.

3

Monosomal karyotype in acute myeloid leukemia: a better indicator of poor prognosis than a complex karyotype.

Breems DA, Van Putten WL, De Greef GE, Van Zelderen-Bhola SL, Gerssen-Schoorl KB, Mellink CH, Nieuwint A, Jotterand M, Hagemeijer A, Beverloo HB, Löwenberg B. Breems DA, et al. Among authors: gerssen schoorl kb. J Clin Oncol. 2008 Oct 10;26(29):4791-7. doi: 10.1200/JCO.2008.16.0259. Epub 2008 Aug 11. J Clin Oncol. 2008. PMID: 18695255

4

Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience.

Tuerlings JH, de France HF, Hamers A, Hordijk R, Van Hemel JO, Hansson K, Hoovers JM, Madan K, Van der Blij-Philipsen M, Gerssen-Schoorl KB, Kremer JA, Smeets DF. Tuerlings JH, et al. Among authors: gerssen schoorl kb. Eur J Hum Genet. 1998 May-Jun;6(3):194-200. doi: 10.1038/sj.ejhg.5200193. Eur J Hum Genet. 1998. PMID: 9781022

5

Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation.

Kok K, Dijkhuizen T, Swart YE, Zorgdrager H, van der Vlies P, Fehrmann R, te Meerman GJ, Gerssen-Schoorl KB, van Essen T, Sikkema-Raddatz B, Buys CH. Kok K, et al. Among authors: gerssen schoorl kb. Eur J Med Genet. 2005 Jul-Sep;48(3):250-62. doi: 10.1016/j.ejmg.2005.04.007. Eur J Med Genet. 2005. PMID: 16179221

6

A third case of de novo partial trisomy 4p.

Oorthuys JW, Gerssen-Schoorl KB, de Pater JM, de France HF. Oorthuys JW, et al. Among authors: gerssen schoorl kb. J Med Genet. 1989 May;26(5):344-5. doi: 10.1136/jmg.26.5.344. J Med Genet. 1989. PMID: 2732997 Free PMC article. No abstract available.

7

Intracranial teratoma with multiple fetuses: pre- and post-natal appearance.

Naudin ten Cate L, Vermeij-Keers C, Smit DA, Cohen-Overbeek TE, Gerssen-Schoorl KB, Dijkhuizen T. Naudin ten Cate L, et al. Among authors: gerssen schoorl kb. Hum Pathol. 1995 Jul;26(7):804-7. doi: 10.1016/0046-8177(95)90232-5. Hum Pathol. 1995. PMID: 7628856

8

An interstitial duplication of chromosome 13q31.3q32.1 further delineates the critical region for postaxial polydactyly type A2.

van der Zwaag PA, Dijkhuizen T, Gerssen-Schoorl KB, Colijn AW, Broens PM, Flapper BC, van Ravenswaaij-Arts CM. van der Zwaag PA, et al. Among authors: gerssen schoorl kb. Eur J Med Genet. 2010 Jan-Feb;53(1):45-9. doi: 10.1016/j.ejmg.2009.11.003. Epub 2009 Nov 23. Eur J Med Genet. 2010. PMID: 19941983

9

A case of de novo interstitial deletion of chromosome 9(p12p13).

Giltay JC, Gerssen-Schoorl KB, van der Wagen A. Giltay JC, et al. Among authors: gerssen schoorl kb. Clin Genet. 1994 Sep;46(3):271-2. doi: 10.1111/j.1399-0004.1994.tb04241.x. Clin Genet. 1994. PMID: 7820945

10

A case of de novo interstitial deletion of chromosome 5(q33q34).

Giltay JC, Gerssen-Schoorl KB, Luitse GH, Dauwerse HG. Giltay JC, et al. Among authors: gerssen schoorl kb. Clin Genet. 1997 Sep;52(3):173-6. doi: 10.1111/j.1399-0004.1997.tb02539.x. Clin Genet. 1997. PMID: 9377807

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